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评估 WISP1 作为老派阿米什人群骨密度的候选基因。

Evaluation of WISP1 as a candidate gene for bone mineral density in the Old Order Amish.

机构信息

School of Medicine, Division of Endocrinology, Diabetes and Nutrition, and Program for Personalized and Genomic Medicine, University of Maryland School of Medicine, Baltimore, MD, 21201, USA.

Department of Orthopedic Surgery, the Second Affiliated Hospital of Chongqing Medical University, Chongqing, 400010, China.

出版信息

Sci Rep. 2018 May 8;8(1):7141. doi: 10.1038/s41598-018-25272-4.

DOI:10.1038/s41598-018-25272-4
PMID:29739999
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5940677/
Abstract

Wnt1-inducible signaling pathway protein-1 (WISP1) is a novel target of the Wnt pathway for modulating osteogenesis and improving bone strength. However, it is not clear if genetic variants in the WISP1 region are associated with bone mineral density (BMD) in human. The aim of this study is to investigate the role of genetic variation in WISP1 gene as a determinant of BMD in 1,510 Old Order Amish (OOA). We performed regional association analysis of 58 tag variants within 5 kb upstream and downstream to WISP1 with BMD and found 5 variants that were associated with BMD at multiple skeletal sites (P values from 2.89 × 10 to 1.62 × 10), with some significant associations even after adjustment for multiple comparisons. To replicate these results in an independent dataset, we performed a look-up of BMD associations with these variants in European ancestry subjects from the large GEFOS Consortium and observed the nominal associations of two of these variants with BMD (P values: 0.031 to 0.048). In conclusion, we have demonstrated that genetic variants surrounding WISP1 are associated with BMD at multiple skeletal sites in the OOA, thus influencing osteoporosis risk. These results support a role for the WISP1 gene on influencing variation in BMD.

摘要

Wnt1 诱导信号通路蛋白-1(WISP1)是调节成骨和提高骨强度的 Wnt 通路的新靶点。然而,WISP1 区域的遗传变异是否与人类的骨密度(BMD)有关尚不清楚。本研究旨在探讨 WISP1 基因遗传变异作为 1510 名老秩序阿米什人(OOA)BMD 决定因素的作用。我们对 WISP1 上下游 5kb 内的 58 个标记变体进行了区域关联分析,发现了 5 个与多个骨骼部位的 BMD 相关的变体(P 值从 2.89×10 到 1.62×10),其中一些甚至在经过多次比较调整后仍具有显著相关性。为了在独立数据集上复制这些结果,我们在来自大型 GEFOS 联盟的欧洲血统受试者中查找了这些变体与 BMD 的关联,观察到其中两个变体与 BMD 的关联具有名义意义(P 值:0.031 至 0.048)。总之,我们已经证明,WISP1 周围的遗传变异与 OOA 中多个骨骼部位的 BMD 相关,从而影响骨质疏松症的风险。这些结果支持 WISP1 基因在影响 BMD 变异方面的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a26/5940677/38b00ead1c84/41598_2018_25272_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a26/5940677/6305a3622098/41598_2018_25272_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a26/5940677/19de327be002/41598_2018_25272_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a26/5940677/47ad241b4e7c/41598_2018_25272_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a26/5940677/38b00ead1c84/41598_2018_25272_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a26/5940677/6305a3622098/41598_2018_25272_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a26/5940677/19de327be002/41598_2018_25272_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a26/5940677/47ad241b4e7c/41598_2018_25272_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a26/5940677/38b00ead1c84/41598_2018_25272_Fig4_HTML.jpg

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本文引用的文献

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